Zinc-iodine battery-capacitor hybrid device with excellent electrochemical performance enabled by a robust iodine host

阴极 电池(电) 超级电容器 材料科学 电容器 储能 电化学 纳米技术 化学工程 碳纤维 功率密度 电气工程 化学 复合数 电压 复合材料 工程类 电极 功率(物理) 物理 物理化学 量子力学
作者
Zhaorui Sun,Xinliang Han,Dewei Wang
出处
期刊:Journal of energy storage [Elsevier BV]
卷期号:62: 106857-106857 被引量:61
标识
DOI:10.1016/j.est.2023.106857
摘要

From both the cost and safety point of view, aqueous rechargeable zinc-ion based electrochemical energy storage devices are highly attractive as a substitute for lithium-ion batteries. The development of zinc‑iodine battery-capacitor hybrid devices (ZIBCHDs) properly integrated with zinc‑iodine batteries (ZIBs) and zinc-ion hybrid capacitors (ZICs) are desired to endure both the large energy density of ZIBs and the high-power density of ZICs. We demonstrated herein an N-doped porous carbon framework (3D) decorated with nanosheets (2D) hybrids can serve as a robust iodine host. Benefitting from its unique 3D2D microstructure, large BET surface area, and abundant surface functional groups, the resulting porous carbon/iodine cathodes can display battery level specific capacity and energy density as well as a supercapacitor level rate capability and cycle stability. The optimized cathode delivers a large reversible specific capacity of 291.5 mAh g−1 at 0.5 A g−1, which is much larger than the corresponding ZIBs (163.8 mAh g−1) and ZICs (148.9 mAh g−1) revealing the broadening potential window can effectively utilize carbon scaffold to further boost the specific capacity. Additionally, the energy storage mechanism was fully explored through a series of ex-situ testing techniques, and a combination of physical/chemical adsorption-desorption and redox reactions mechanism has been proposed.
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